Human Disease and Mouse Model Detail
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Human Disease
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Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation; MCLMR
OMIM ID: 152950
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Synonyms
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Cdmmr Syndrome;
Lymphedema and Retinal Folds with Microcephaly and Microphthalmos;
Lymphedema, Microcephaly, Chorioretinopathy Syndrome;
Microcephaly and Chorioretinopathy with or without Mental Retardation, Autosomal Dominant;
Microcephaly, Lymphedema, Chorioretinal Dysplasia Syndrome;
Mlcrd Syndrome
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Kif11
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KIF11*
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1:1 Homology
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Analysis Tools